Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1990318762
Device Listing 1990318762
Listing Summary
#
Listing key
1990318762
Premarket submission
K223905
Device
Vivio® LVEDP System
Applicant
Avicena, LLC
Product code
QUO
Decision date
2023-10-06
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
321106
3018772859
3018772859
AVICENA LLC DBA VENTRIC HEALTH
1
N
2026-01-01
117 E Colorado Blvd., Suite 510 Pasadena CA US 91105